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CTGA Database Listing
Arab Genomic Studies
Records found: 2794 Sort by:
  • Vascular Malformation, Primary Intraosseous
    OMIM # 606893
    Vascular Malformation Osseous, VMOS, Hemangioma, Intraosseous, IOH
  • Polymicrogyria, Bilateral Frontoparietal
    OMIM # 606854
    BFPP, Cerebellar Ataxia with Neuronal Migration Defect,
  • Stroke, Susceptibility to, 1
    OMIM # 606799
    STRK1
  • Anorexia Nervosa, Susceptibility to, 1
    OMIM # 606788
    ANON1, AN
  • GLUT1 Deficiency Syndrome 1
    OMIM # 606777
    GLUT1DS1, Glucose Transport Defect, Blood-Brain Barrier, GLUT1 Deficiency Syndrome 1, Autosomal Recessive
  • Parkinson Disease 9
    OMIM # 606693
    KRS, Parkinson Disease 9, PARK9, Pallidopyramidal Degeneration with Supranuclear Upgaze Paresis and Dementia, KRPPD,
  • Spinocerebellar Ataxia 15
    OMIM # 606658
    SCA15, Spinocerebellar Ataxia 16, SCA16,
  • Muscular Dystrophy, Congenital, 1C
    OMIM # 606612
    MDC1C
  • Ichthyosis, Lamellar, 5
    OMIM # 606545
    LI5, Lamellar Ichthyosis, Type 5
  • Epileptic Encephalopathy, Lennox-Gastaut Type
    OMIM # 606369
    Encephalopathy of Childhood
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